Thought I'd make it official that the podcast is on a bit of a break.
The plan was to put out a mini episode in the summer and then get back into it in September, but yeah, not so much. #chronicillnesslife
Soooooooo, another way of getting oxygenated in addition to ventilators might me coming someday (not tested in humans yet) .... I'm a little weirded out, but less lung damage sounds good.
https://t.co/fhNJCfEglK
This still haunts me: when someone said my #disability is because my parents or grandparents did something very bad. No one's said it's my fault, but sometimes, the vibe is in the air. Have you ever felt or heard this?
Thanks to the wonderful @TheDisabledDiva for the graphic.
Nausea: Sorry I've been giving you such a hard time. You doing okay now?
Me: Yeah, I managed to eat something a while ago.
Nausea: 😈
#migrainelife#chronicillnesslife
@bennessb And anyone treating people with the condition would have to wear the simulator for a month. I want them not just to know what it's like, but to KNOW.
@HSDExplainsALot @bennessb It doesn't help me during an attack, I'm team distraction then. Meditating when the pain is bad just makes the pain louder for me. But between attacks I do find it helpful. It gives my brain space to notice warning signs much earlier.
I was going to rant that if I can smell you from social distancing away, then it's too much perfume! #migrainetrigger
But maybe they were people that can't smell cause of covid. So now it's a #PSA.
PUT DOWN THE PERFUME! You're destroying all of us with #migraine Please Stop.